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ECI Therapeutics develops biologic products using a proprietary platform that combines human platelet-rich plasma-derived growth factors with chitosan or hyaluronic acid excipients. The lead indication, neurotrophic keratitis, has received orphan drug designation from the FDA. The company aims to address significant unmet needs in ophthalmology—especially rare corneal diseases—and wound care by providing safer, more effective alternatives to current treatments. Clinical results are pending; first Phase II trial anticipated in 2026.
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